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Ritter 003-1030-00
Ritter 003-1030-00
Installation Important
Information
& Operation Page 2
Manual Installation
Page 4
Description
Controls &
Indicators
D R Page 9
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Limited
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MODEL NUMBER
SERIAL NUMBER
MA439101
CONTENTS
IMPORTANT INFORMATION ........................................................................................................ 2
Scope and Purpose of This Manual ...................................................................................... 2
Intended Use of Product........................................................................................................ 2
Safety Instructions................................................................................................................. 2
Explanation of Safety Symbols and Notes ............................................................................ 3
Transportation and Storage Conditions ................................................................................. 3
INSTALLATION.............................................................................................................................. 4
Location Requirements For Sterilizer .................................................................................... 4
Re-Location Requirements For Sterilizer .............................................................................. 5
Electrical Requirements ........................................................................................................ 6
DESCRIPTION............................................................................................................................... 6
Operational Features............................................................................................................. 6
Mechanical Features ............................................................................................................. 7
Safety Features ..................................................................................................................... 7
COMPONENTS OVERVIEW ......................................................................................................... 8
CONTROLS & INDICATORS ........................................................................................................ 9
OPERATION ................................................................................................................................ 11
Recommended Steam Sterilization Monitoring Program .................................................... 12
Sterilizer Preparation Before Operation............................................................................... 12
Cleaning Instruments .......................................................................................................... 13
Guidelines For Loading Trays .............................................................................................. 14
Operation............................................................................................................................. 16
Standard Cycle Parameters ................................................................................................ 19
List of Authorized Accessories ............................................................................................ 19
OPERATOR MAINTENANCE ..................................................................................................... 20
Daily .................................................................................................................................... 20
Weekly................................................................................................................................. 20
Monthly................................................................................................................................ 20
Quarterly ............................................................................................................................. 23
Toubleshooting Guide.......................................................................................................... 24
Error Code Guide ................................................................................................................ 26
CALLING FOR SERVICE ............................................................................................................ 28
SPECIFICATIONS ....................................................................................................................... 29
LIMITED WARRANTY ................................................................................................................. 29
PRINTER INSTALLATION AND OPERATION ............................................................................ 30
Installing the Printer ............................................................................................................ 31
Operating the Printer........................................................................................................... 34
Inserting the Paper Roll....................................................................................................... 34
About the Cartridge Ribbon................................................................................................. 35
Installing a New Cartridge Ribbon....................................................................................... 36
Removing the Paper Roll..................................................................................................... 37
Power Up Message ............................................................................................................. 37
Printer Tape Description ...................................................................................................... 37
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Important
IMPORTANT INFORMATION
Information
Scope and Purpose of This Manual
This manual provides complete instructions for the installation, operation, and
normal care of the M11 UltraClave™ Steam Sterilizer. It is intended that this
manual be used by all personnel operating the sterilizer or performing operator
level maintenance. No repair information is included in this manual as no re-
pairs are authorized at the operator level.
Safety Instructions
The primary concern of Midmark is that this equipment is operated and main-
tained with the safety of the patient and staff in mind. To assure safer and more
reliable operation:
• Read and understand this manual before attempting to install or operate the
sterilizer.
• Assure that appropriate personnel are informed on the contents of this man-
ual; this is the responsibility of the purchaser.
• Assure that this manual is located near the sterilizer, or if possible, perma-
nently affixed to the sterilizer.
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WARNING
Indicates a potentially hazardous situation which, if not avoid-
ed, could result in death or serious injury.
CAUTION
Indicates a potentially hazardous situation which, if not avoided,
may result in minor or moderate injury. It may also be used to alert
against unsafe practices.
EQUIPMENT ALERT
Indicates an imminently or potentially hazardous situation which, if
not avoided, will or may result in serious, moderate, or minor
equipment damage.
NOTE
Amplifies an operating procedure, practice, or condition.
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INSTALLATION
Location Requirements For Sterilizer
Installation
DANGER
Do not operate this sterilizer in areas where flammable anes-
thetics are used or stored. An explosion could occur, caus-
ing personal injury.
D
C
A
MA439500
Support Surface (A) - Sterilizer must be placed on a level surface to ensure that
the chamber will fill correctly. Improper water level in the chamber could cause
a sterilizer malfunction.
Support Surface Material (B) - Formica, stainless steel, or other water and heat
resistant material. Heat from bottom of sterilizer could reach 71°C (160° F) on
the support surfaces for short periods of time.
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Distance To Side Wall (D) - If the sterilizer is located next to side walls, there
should be no less than 51 mm (2 in) clearance between the side of the sterilizer
Installation
and the wall.
Distance Above Sterilizer (E) - If the sterilizer is to be located beneath wall cabi-
nets or shelves, the underside of the cabinets or shelves should be at least 584
mm (23 in) above the support surface, to provide access to the top inspection
cover and to allow for changing the printer paper roll.
Location On Support Surface - The front of the sterilizer should be located near
the front of the support surface so water can be easily drained from the tube into
a container.
2. Drain water from reservoir or take care not to tip the sterilizer, which will
allow water to spill from reservoir.
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Electrical Requirements
WARNING
Use 220 - 240 VAC, 50/60 HZ alternating current only for 230
VAC models and 90 - 110 VAC, 50/60 HZ alternating current
Installation
only for 100 VAC models. Failure to do so could result in electrical
shock to personnel and will result in damage to sterilizer.
NOTE
Grounding reliability can only be achieved if this unit is connected to a match-
ing three-pronged, grounded, isolated, correctly polarized receptacle.
The electrical rating for the 230 VAC unit is 230 VAC, 50/60 Hz, 10 amps. The
electrical rating for the 120 VAC unit is 120 VAC, 60 Hz, 15 amps. The electrical
rating for the 100 VAC unit is 100 VAC, 50/60 Hz, 20 amps. The three-pronged
grounding plug on the sterilizer power cord must be plugged into a matching
three-pronged, grounded, isolated, correctly polarized receptacle. Check the
serial number label on the back panel of the sterilizer to verify the voltage rating
for the unit.
DESCRIPTION
Operational Features
The M11 UltraClave™ sterilizers . . .
Mechanical Features
Installation
The M11UltraClave™ sterilizers . . .
• have a tray rack which can hold two small and two large trays. The tray rack
can be removed for periodic cleaning of the chamber, tray plate, tray rack,
and filter. Description
• have an optional printer which provides a permanent record of actual expo-
sure times and temperatures.
• have a removable power supply cord (100 and 230 VAC units only).
• have a two gaskets in the door; a dam gasket and a door gasket which can
easily be replaced by operator in seconds.
Safety Features
The M11UltraClave™ sterilizers . . .
• have a door stop which prevents the door from opening fully if there is a
slight residual pressure in the chamber when the door handle is operated.
The door stop also retains the door in a partially open position during the
drying cycle.
• have a door closed switch which is used to signal the sterilizer that the
door is completely closed. This switch is activated just as the door becomes
fully closed. An audible signal will sound and the “Door Ajar” light will flash if
the door is not fully closed.
• have a water low indicator which signals the operator if there is insufficient
water to fill the chamber to the proper level. An audible signal will sound and
the “Water Low” light will flash if the reservoir needs to be refilled with water.
• have their chamber temperature monitored during a cycle to prevent an
overheat condition. If chamber temperature reaches or exceeds 146°C
(295°F), power to the sterilizer is cut off.
• have a pressure relief valve which opens to provide backup protection to
reduce chamber pressure in the event that the chamber steam pressure
exceeds the allowable limit. Released steam is directed out of the bottom of
the unit’s cabinet. An access cover is located on the top cover for relief valve
operational checks.
• have a fault detection circuit which monitors all functions of the sterilizer
during a cycle. If a fault occurs during a cycle, the sterilizer monitoring cir-
cuitry will stop the cycle, sound an audible signal, and light a flashing error
lamp.
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COMPONENTS OVERVIEW
The illustration below shows the location of the sterilizer’s major components
and the chart below provides their descriptive name.
8 3
1 6
Components
Overview
5
4
MA439900
DESCRIPTION OF COMPONENTS
1. Access Cover 5. Door and Dam Gaskets
2. Reservoir Lid 6. Display / Control Pad
3. Printer (Optional) 7. Wire Tray Rack and Tray Plate
4. Level Indicator / Reservoir 8. Pressure Relief Valve
Drain Tube
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1 3 4 5 6 7 8 9
PRESSURE (PSI)
UNWRAPPED POUCHES LIQUIDS PACKS START STOP ON/STANDBY
Components
2 10 12 14 16 Overview
11 13 15
17 Controls &
Indicators
18
20
19
MA439400
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OPERATION
DANGER
Do not use this sterilizer in an explosive or oxygen-rich atmo-
sphere, or where flammable anesthetics are stored. To do so
could result in an explosion or fire.
EQUIPMENT ALERT
For optimal sterilizer performance, allow the sterilizer to reach
room temperature before operating.
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Follow the appropriate agency (state dental or medical board) for sterilization
monitoring guidelines for your office. Additional information can also be ob-
tained from CDC, AAMI, OSAP, and ADA regarding monitoring programs or oth-
er sterilization issues.
1. Locate the sterilizer and plug in its power cord in accordance with the Instal-
lation instructions contained earlier in this manual.
EQUIPMENT ALERT
Use only distilled or demineralized water. Normal tap water con-
tains minerals, especially chlorides, which have corrosive effects
on stainless steel. Failure to use distilled or demineralized water may cause
serious deterioration and premature failure of the stainless steel chamber
which could result in serious injury or death.
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4. Dry instruments.
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The M11 sterilizers are equipped with two large and two small trays to maximize
the number of items that can be processed at one time and provide separation
for better steam flow and penetration. Four properly loaded trays, as noted in
the chart on page 15 (two large and two small), is the maximum load for the
M11 sterilizers.
General Guidelines
• Sterilize jointed instruments in an open position.
• Place all containers so the opening allows steam to enter and air to leave the
container (containers are usually positioned on their side or with the opening
Operation
tilted slightly down).
• Pouch or wrap items to preserve sterility after processing. Use only protec-
tive coverings designed and recommended for use with steam sterilization.
• Do not wrap items too tightly. Steam penetration will be affected if an item
has excessive wrapping.
• Do not stack trays on one another. Using Midmark’s standard tray rack and
trays provides proper tray spacing.
• Position loads on trays with appropriate space between items. Adequate
space is required between items to allow proper steam flow and drying.
• Place unwrapped items on a towel or absorbent paper.
• Vented liquid containers should not be filled to more than 75% of their
capacity to allow for fluid expansion and to prevent overflow. Depending on
the user’s desired results, many different container styles may be accept-
able. Careful consideration of the liquid to be sterilized should guide the
user in selection and use of appropriate containers and closures. Always
consult the liquid and/or container manufacturer for information on steriliza-
tion. Not recommended for sterilization of liquids intended for direct
patient contact.
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Loads Including Dental Handpieces and/or Instruments
NOTE
Dental handpieces should only be sterilized when placed in a pouch and in
the POUCHES cycle. Only one handpiece should be placed in each pouch.
The maximum M11 load shall be nine handpieces (in the pouch rack) and 75 in-
struments. Other combinations of fewer handpieces and items can be pro-
cessed in a single load if that allows for efficient sterilization. If a load
surpasses these limits, we recommend dividing the load and running multiple
cycles. Listed below are the maximum recommended loads for each tray:
Maximum Capacities
M11 Large /
Load Type M11 Small Tray Sterilizer Total
Deep Tray
Solid Items 45 instruments - 1224 30 instruments - 816 150 instruments - 4.1
grams (2.7 lbs.) or grams (1.8 lbs.) or kg (9.0 lbs) or
Handpieces 9 in rack or 9 in rack or 9 handpieces in rack
and 75 instruments or
Liquids (†) 3 - 198 ml (6.76 oz) 2 - 198 ml (6.76 oz) 3 - 198 ml (6.76 oz)
containers or containers or containers or
† Not recommended for sterilization of liquids intended for direct patient con-
tact.
‡ Packs to have a minimum of 1/4 in. (6.3 mm) space between each other and
away from all sterilizer surfaces.
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Operation
WARNING
Do not use this sterilizer in an explosive or oxygen-rich atmo-
sphere, or where flammable anesthetics are stored. To do so
could result in an explosion or fire.
Do not use this sterilizer for sterilizing volatile substances or for any
purpose other than its intended design. Burns and toxic or explosive
conditions could result.
Clean and dry instruments before putting them into the sterilizer.
Incomplete and improper cleaning of instruments will impede steriliza-
tion and will result in unsterile instruments which could lead to per-
sonal injury or death.
Do not force door handle at any time. Chamber pressure may cause
door to open with extreme force. If the door handle does not move
freely, allow unit to cool and depressurize for 40 minutes before open-
Operation
ing door. Failure to adhere could result in serious personal injury or
death.
EQUIPMENT ALERT
Do not use toweling or packaging which may contain chlorine
bleach residue. Doing so could result in trays and/or chamber
rusting or discoloring. In extreme cases, the life of the chamber may be sig-
nificantly shortened.
NOTE
Use sterility monitors with each sterilization load. Also, if a sterilizing cycle is
terminated prematurely, reprocess the instruments to ensure the sterility of
the load.
Refer to the following steps for a detailed description of the program operating
procedures:
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hide
3 5 6 8 9
PRESSURE (PSI)
UNWRAPPED POUCHES LIQUIDS PACKS START STOP ON/STANDBY
7 1
4
2 MA439200
NOTE
Before operating the sterilizer, be sure the door handle is completely de- Operation
pressed (latched). If the handle is not fully latched, the sterilizer will alert the
operator with an audible beep and will not start until the door handle is
latched.
2. Close and latch the door; the sterilizer will not operate unless the door is
closed.
EQUIPMENT ALERT
Processing goods using an incorrect sterilization program could
result in unsterile goods and may damage instruments. Consult
with your supply manufacturer for specific sterilization instructions.
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WARNING
Keep clear when the door is ready to open. Five series of
three audible beeps will be heard prior to partial door open-
ing. Leave door in this position until steam dissipates. Failure to do so
could result in severe burns from steam being released.
Operation CAUTION
The processed load and metal inner surfaces will be hot at the
completion of the drying phase. Avoid contact. Failure to do so
could result in serious burns.
NOTE
The sterility of wrapped or packed instruments cannot be ensured unless the
wrapped or packed instruments are allowed to dry fully.
• Leave the sterilization load in the chamber to dry or remove the steriliza-
tion load from the chamber if drying is not necessary.
• When the 30 minute drying phase is complete, the sterilizer signals the
operator that the drying phase is complete with five series of three audible
beeps and the COMPLETE lamp (9) illuminates to indicate that the pro-
gram cycle is complete.
• Remove the sterilizer load from the chamber.
5. Press the ON / STANDBY button (1) to return the sterilizer to the STANDBY
mode or if additional sterilization program cycles are desired, restart the
sterilizer at this time.
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Liquids 121°C (250°F) / Liquids or gels that could boil over with
104 kPa (15 psi) rapid depressurization. Cycle includes
for 30 minutes special vent and dry functions. Not rec-
ommended for sterilization of liquids
intended for direct patient contact.
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OPERATOR MAINTENANCE
It is the responsibility of the user to establish a periodic maintenance procedure
to assure correct operation of the equipment and reliable sterilization of the
loads. Contact your local distributor or representative to develop a program for
planned maintenance.
Daily
1. Clean External Surfaces - Wipe with a soft dry cloth and wash occasionally
with a damp cloth and mild soap or detergent.
WARNING
Make sure that the unit is cool when cleaning the door gasket
and any mating surfaces. Failure to do so could result in seri-
ous burns to hands.
2. Clean Sterilizer Door Gasket - Clean door gasket and mating surface with a
damp cloth. Examine gasket for possible damage that could prevent a good
sealing surface.
Weekly
1. Clean Chamber and Trays - The sterilizing chamber and instrument trays
should be cleaned weekly. First, drain the water from the reservoir. A drain
tube is located on the front of the unit for draining. Wash the inside of the
chamber and the trays with mild soap or Speed-Clean and distilled or dem-
ineralized water. Refill the reservoir with distilled or demineralized water.
Monthly
1. Flush the System - To protect the intricate parts of the unit, the system must
be flushed once a month with Speed Clean Sterilizer Cleaner:
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(a) Drain reservoir and fill with clean, distilled water then add one ounce of
Speed Clean Sterilizer Cleaner to a cool chamber.
(b) Run one 30 minute cycle (PACKS) at 121°C (250°F). Instruments must
not be sterilized while cleaning the sterilizer.
(c) Drain reservoir fill with clean distilled or demineralized water and run one
3 minute cycle (UNWRAPPED) at 132°C (270°F).
(f) Re-install the tray rack (1) and tray plate (2) in the chamber as follows: Operator
Position the two rear posts of tray rack in rack holes (A) of tray plate. Maintenance
Then, hold front end of tray rack at approximately a 30° angle from the
tray plate. Then, insert rear end of tray rack and tray plate as an assem-
bly in chamber (3). Push tray rack and tray plate into chamber com-
pletely. Re-install the trays.
2. Perform Pressure Relief Valve Check - The pressure relief valve must be
checked each month by a qualified person to be sure that the relief valve is
functioning properly:
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(c) When the “heat up” portion of the cycle is complete and the elapsed time
is being counted down on the display panel, pull upward on wire ring (A)
of pressure relief valve (2) with a screwdriver for approximately 3 sec-
onds; steam should discharge freely from beneath the rear of the unit.
NOTE
If the pressure relief valve does not close completely when the wire ring is re-
leased, pull the wire ring again and release it quickly so the valve snaps back
into position. Do this until the valve seats properly.
Operator
(d) Release the wire ring of pressure relief valve (2). The steam should vent
Maintenance
out of the pressure relief valve until the wire ring is released. When the
wire ring is released, the valve should seat, stopping the release of
steam.
(f) If excessive force is required to open pressure relief valve (2) or pres-
sure relief valve will not reseat properly, the pressure relief valve must be
replaced (See Calling For Service later in this manual).
(g) Install top inspection cover (1).
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NOTE
If the filter cannot be cleaned ef-
fectively, the filter must be re-
placed. MA438800
(c) Grasp the filter (1) and gently pull upwards while twisting slightly (a pair
of pliers may be used if filter is stuck). The filter may be cleaned with
mild soap and distilled or demineralized water. A small stiff bristled
brush or ultrasonic cleaner may be helpful to remove foreign objects
from the filter surface. Rinse the filter with distilled or demineralized
water.
EQUIPMENT ALERT
Do not operate the sterilizer without the filter in place. Doing so
could result in the sterilizer malfunctioning. Operator
Maintenance
(d) Replace the filter (1) by inserting the filter into the hole in the chamber
bottom and pressing downwards while twisting slightly.
Quarterly
1. Remove and Clean Door Gasket - the door gasket and dam gasket must be
removed and checked and the gasket housing channel must be cleaned as
follows:
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Troubleshooting Guide
Use the following table to assist in correcting minor problems with the sterilizer.
Operator Troubleshooting Guide
Maintenance
Problem Possible Cause Solution
WATER LOW lamp in not enough water in add distilled or
on. reservoir tank to fill demineralized water to
chamber. reservoir tank.
DOOR AJAR lamp is on. Chamber door is not fully Close the door properly and
closed and / or latched. make sure the door is fully
latched.
ERROR lamp is on. _ See Error Code Guide for a
detailed explanation
Steam is escaping from pressure relief valve was Reseat the pressure relief
the pressure relief valve. not properly reseated after valve (see Perform Pressure
pressure relief valve Relief Valve Check under
inspection Monthly maintenance in this
manual).
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Error Code 8 door did not open at end of make sure the tray rack is
(door malfunction) cycle. pushed all the way back into
the chamber and is not
making contact with door.
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SPECIFICATIONS
Physical Dimensions:
Overall Length ................................. 559 mm (22 in)
Overall Width................................... 457 mm (18 in)
Overall Height.................................. 445 mm (17.5 in)
Counter Area................................... 457 mm x 406 mm (18 x 16 in)
Chamber ......................................... 279 mm Diameter x 457 mm depth
(11 in Diameter x 18 in depth)
Large Trays (2) ................................ 381 mm x 152 mm x 25 mm
(15 in x 9 in x 1 in)
Small Trays (2) ................................ 381 mm x 152 mm x 25 mm
(15 in x 6 in x 1 in)
Weight:
Empty Reservoir.............................. 45 Kgs (95 lbs)
With Shipping Carton ...................... 48 kgs (105 lbs)
Water Reservoir Capacity............. Approximately 4.54 Liters to Full Mark
(1.2 gallons)
Electrical Requirements:
NOTE: A separate (dedicated) circuit is recommended for this sterilizer. The
sterilizer should not be connected into an electrical circuit with other appliances
or equipment unless the circuit is rated for the additional load.
100 VAC, 50/60 Hz Model ............... 20 AMP Circuit, Single Phase
120 VAC, 60 Hz Model .................... 15 AMP Circuit, Single Phase
220-240 VAC, 50/60 Hz Model ........ 10 AMP Circuit, Single Phase
Maximum Power Consumption:
Operator
100 VAC, 50/60 Hz Model ............... 1425 Watts, 14.2 A @ 100V Maintenance
120 VAC, 60 Hz Model .................... 1425 Watts, 11.9 A @ 120 V
220-240 VAC, 50/60 Hz Model ........ 1500 Watts, 6.3 A @ 240 V
Chamber Pressure at
132°C (270°F) ................................. 215 kPa (31 psi) Calling For
Service
Safety Valve Setting ...................... 276 kPa (40 psi)
Certifications ................................. ISO-9001 Certified
SCOPE OF WARRANTY
Midmark Corporation (“Midmark”) warrants to the original purchaser its new Alter-
nate Care products and components (except for components not warranted under
“Exclusions”) manufactured by Midmark to be free from defects in material and Limited
workmanship under normal use and service. Midmark’s obligation under this war- Warranty
ranty is limited to the repair or replacement, at Midmark’s option, of the parts or the
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products the defects of which are reported to Midmark within the applicable warranty
period and which, upon examination by Midmark, prove to be defective.
EXCLUSIONS
This warranty does not cover and Midmark shall not be liable for the following: (1)
repairs and replacements because of misuse, abuse, negligence, alteration, acci-
dent, freight damage, or tampering; (2) products which are not installed, used, and
properly cleaned as required in the Midmark “Installation” and or “Installation / Oper-
ation Manual for this applicable product. (3) products considered to be of a consum-
able nature; (4) accessories or parts not manufactured by Midmark; (5) charges by
anyone for adjustments, repairs, replacement parts, installation, or other work per-
formed upon or in connection with such products which is not expressly authorized
in writing in advance by Midmark.
EXCLUSIVE REMEDY
Midmark’s only obligation under this warranty is the repair or replacement of defec-
tive parts. Midmark shall not be liable for any direct, special, indirect, incidental,
exemplary, or consequential damages or delay, including, but not limited to, dam-
ages for loss of profits or loss of use.
NO AUTHORIZATION
No person or firm is authorized to create for Midmark any other obligation or liability
in connection with the products.
SF-1487 REV. A1
Limited
Warranty
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1 3
5 2
4 6
MA438400
3. Remove two screws (3) and printer cover plate (4) from top cover (2). Store
the two screws and printer cover plate in the event that the printer is
removed and these parts are needed again.
4. Remove two screws (5) from top cover (2).
5. Pull outward and down on the top edge of the right hand side panel (6) and
remove right hand side panel from sterilizer.
Limited
Warranty
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3 2
5
4
1
D
EE
/F
ON
F
OF
7. Route PCB printer harness (1) through harness clip (3) to prevent harness
from contacting hot pressure relief valve.
8. Place the printer (4) on the top cover in the recessed area.
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10. Insert two tabs (A) of right hand side panel (1) into two slots (B) of base (2).
3 4
1
B C
6
2
A
4
MA438600
11. Raise top edge of right hand side panel (1) into position under top cover (4)
and secure using two screws (3).
12. Install top inspection cover (5) on top cover (4), making sure PCB printer
harness (6) is routed into harness cutout (C) of top inspection cover.
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ON
printer is a rocker type switch. OF
F
F
OF
erly. When turning the printer
OFF, wait at least 3 seconds be-
fore turning the printer back on.
MA439600
2. Unroll 5 to 7.5 cm (2 to 3 B
in.) of paper (1). A
3. Cut a straight edge on the
paper (1) if it is torn or 2
jagged; this will facilitate
the entry of paper into the
4
printer.
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6. While holding the paper (1) in place, press the right side (B) of the switch to
the ON / FEED position and hold. The printer will activate and a rubber roller
will put the paper into the printer compartment. Continue to hold the switch
down until the paper emerges from the top of the printer mechanism. Then,
when 2.5 cm (1 in.) of paper has emerged from the top of the printer, release
the switch.
7. Pull the paper (1) through the printer until 5 to 7.5 cm (2 to 3 in.) of paper is
exposed.
8. Put the paper spindle (3) into the paper roll and place the roll with the spindle
onto the grooves (4) at the back of the printer.
9. Turn the paper roll so as to take up the slack in the paper feeding to the
printer. Make sure the roll of paper turns freely. If it does not turn freely, the
paper will jam and possibly damage the printer mechanism.
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H
EJECT
PUS
ED
D
FE
F/E
O/N
NOTE FFF
OO
FON
5. Install the new ribbon cartridge (2). Be sure the ribbon is inserted in front of
the paper and the ribbon is flat against the paper. Press the ribbon cartridge
(2) downward until it snaps into place.
6. Turn the knob (3) on the ribbon cartridge (marked by an arrow) clockwise to
stretch the ribbon so it is tight.
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Before removing the paper roll, advance the paper about 2.5 cm (1 in.) beyond
the paper cutter by pressing down and holding the switch to the ON / FEED po-
sition. Lift the paper roll away from the printer housing, and with a scissors, cut
the paper roll feeding to the printer. Try to make the cut as straight as possible
to facilitate the next reloading of the paper. Now, pull the remaining paper
through the printer mechanism.
Power Up Message
When the printer is first turned on, it prints the word READY to assure the oper-
ator that its built in microprocessor is working properly. When turning the printer
OFF, wait at least 3 seconds before turning the printer back on.
Set Temperature
Set Time
Run Number
Date: a blank line is printed so that the date can be recorded on the printer tape.
The printer will print the chamber temperature, the chamber pressure, and the
time elapsed in two (2) minute increments during the heat up phase.
During the actual Sterilization Phase of the program cycle, the printer will record
the chamber temperature, chamber pressure, and the time elapsed for each
minute of the program cycle.
When the sterilizer has completed the Sterilization Phase of the program cycle,
the printer will print the word VENT to show that the steam pressure was ex-
hausted from the chamber.
When the sterilizer has completed the Drying Phase of the program cycle, the
word COMPLETE will be printed to show that the sterilizer has completed the
sterilization program cycle.
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BEGIN
DATE
HEAT UP
STERILIZE
VENT
COMPLETE
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NOTES:
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NOTES:
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Midmark Corporation
60 Vista Drive
P.O. Box 286 003-1030-00 Rev. F (3/03)
Versailles, Ohio 45380-0286
937-526-3662
Fax 937-526-5542
midmark.com